2,3,4,6-Tetra-O-benzoyl-α-D-glucopyranosyl p-Trifluoromethylbenzylthio-N-(p-trifluoromethylphenyl)formimidate

≥96%

Reagent Code: #103665
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CAS Number 428816-48-2

science Other reagents with same CAS 428816-48-2

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scatter_plot Molecular Information
Weight 957.89 g/mol
Formula C₅₀H₃₇F₆NO₁₀S
badge Registry Numbers
MDL Number MFCD06797174
inventory_2 Storage & Handling
Storage -20°C

description Product Description

This chemical is primarily utilized in the synthesis of complex carbohydrates and glycoconjugates, playing a critical role in glycosylation reactions. Its structure, featuring multiple benzoyl groups and a trifluoromethylphenyl moiety, enhances its stability and reactivity, making it suitable for creating glycosidic bonds with high selectivity. It is particularly valuable in the preparation of oligosaccharides and glycoproteins, which are essential in biological studies and pharmaceutical development. Additionally, its application extends to the field of glycobiology, where it aids in understanding carbohydrate-protein interactions and developing carbohydrate-based therapeutics, such as vaccines and enzyme inhibitors.

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿12,510.00

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2,3,4,6-Tetra-O-benzoyl-α-D-glucopyranosyl p-Trifluoromethylbenzylthio-N-(p-trifluoromethylphenyl)formimidate
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This chemical is primarily utilized in the synthesis of complex carbohydrates and glycoconjugates, playing a critical role in glycosylation reactions. Its structure, featuring multiple benzoyl groups and a trifluoromethylphenyl moiety, enhances its stability and reactivity, making it suitable for creating glycosidic bonds with high selectivity. It is particularly valuable in the preparation of oligosaccharides and glycoproteins, which are essential in biological studies and pharmaceutical development. Ad

This chemical is primarily utilized in the synthesis of complex carbohydrates and glycoconjugates, playing a critical role in glycosylation reactions. Its structure, featuring multiple benzoyl groups and a trifluoromethylphenyl moiety, enhances its stability and reactivity, making it suitable for creating glycosidic bonds with high selectivity. It is particularly valuable in the preparation of oligosaccharides and glycoproteins, which are essential in biological studies and pharmaceutical development. Additionally, its application extends to the field of glycobiology, where it aids in understanding carbohydrate-protein interactions and developing carbohydrate-based therapeutics, such as vaccines and enzyme inhibitors.

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